| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587777042 | 0.882 | 0.040 | 8 | 144096615 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs104894006 | 0.925 | 0.040 | 7 | 44149992 | stop gained | G/A;T | snv | 1.2E-05 | 2 | ||
| rs1564865302 | 0.925 | 0.040 | 11 | 17387395 | missense variant | G/A | snv | 2 | |||
| rs8066560 | 0.925 | 0.040 | 17 | 17824729 | intron variant | A/G | snv | 0.64 | 2 | ||
| rs10139403 | 1.000 | 0.040 | 14 | 100728224 | intron variant | A/G | snv | 0.62 | 1 | ||
| rs1018185646 | 1.000 | 0.040 | 20 | 44428455 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs1410713 | 1.000 | 0.040 | 20 | 3079704 | downstream gene variant | A/C | snv | 0.62 | 1 | ||
| rs1447680989 | 1.000 | 0.040 | 2 | 27501147 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs2282018 | 1.000 | 0.040 | 20 | 3084303 | intron variant | C/T | snv | 0.60 | 1 | ||
| rs2770381 | 1.000 | 0.040 | 20 | 3081340 | downstream gene variant | A/C | snv | 0.35 | 1 | ||
| rs6084264 | 1.000 | 0.040 | 20 | 3089925 | upstream gene variant | T/C | snv | 0.58 | 1 | ||
| rs746913146 | 1.000 | 0.040 | 7 | 44149816 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs750931344 | 1.000 | 0.040 | 12 | 46769424 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs755498926 | 1.000 | 0.040 | 7 | 44145228 | missense variant | T/C | snv | 4.1E-06 | 1 | ||
| rs775776658 | 1.000 | 0.040 | 11 | 17474926 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 2.0E-05 | 1 | ||
| rs137853240 | 0.807 | 0.080 | 12 | 120994405 | missense variant | G/A | snv | 1.4E-05 | 8 | ||
| rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 7 | ||
| rs1272388614 | 0.851 | 0.080 | 11 | 17395658 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 5 | |
| rs146488435 | 0.851 | 0.080 | 17 | 63533914 | missense variant | C/G;T | snv | 8.0E-06; 6.4E-05 | 5 | ||
| rs12836771 | 0.882 | 0.080 | X | 114650913 | intron variant | A/G | snv | 0.12 | 4 | ||
| rs193922331 | 0.882 | 0.080 | 7 | 44147726 | missense variant | A/G | snv | 7.0E-06 | 4 | ||
| rs4436578 | 0.925 | 0.080 | 11 | 113436043 | intron variant | C/T | snv | 0.73 | 4 | ||
| rs764232985 | 0.851 | 0.080 | 7 | 44153381 | missense variant | C/G;T | snv | 4.0E-06 | 4 | ||
| rs1057524902 | 0.882 | 0.080 | 7 | 44145495 | splice donor variant | A/T | snv | 3 | |||
| rs1057524904 | 0.882 | 0.080 | 7 | 44147765 | missense variant | G/A | snv | 3 |